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Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number.
Koller A, Filosi M, Weissensteiner H, Fazzini F, Gorski M, Pattaro C, Schönherr S, Forer L, Herold JM, Stark KJ, Döttelmayer P, Hicks AA, Pramstaller PP, Würzner R, Eckardt KU, Heid IM, Fuchsberger C, Lamina C, Kronenberg F. Koller A, et al. Sci Rep. 2024 Jan 24;14(1):2083. doi: 10.1038/s41598-024-52373-0. Sci Rep. 2024. PMID: 38267512 Free PMC article.
Hypertrophic cardiomyopathy is characterized by alterations of the mitochondrial calcium uniporter complex proteins: insights from patients with aortic valve stenosis versus hypertrophic obstructive cardiomyopathy.
Paar V, Haslinger M, Krombholz-Reindl P, Pittner S, Neuner M, Jirak P, Kolbitsch T, Minnich B, Schrödl F, Kaser-Eichberger A, Kopp K, Koller A, Steinwender C, Lichtenauer M, Monticelli FC, Seitelberger R, Hoppe UC, Dinges C, Motloch LJ. Paar V, et al. Among authors: koller a. Front Pharmacol. 2023 Nov 22;14:1264216. doi: 10.3389/fphar.2023.1264216. eCollection 2023. Front Pharmacol. 2023. PMID: 38074139 Free PMC article.
Meta-GWAS on PCSK9 concentrations reveals associations of novel loci outside the PCSK9 locus in White populations.
Kheirkhah A, Schachtl-Riess JF, Lamina C, Di Maio S, Koller A, Schönherr S, Coassin S, Forer L, Sekula P, Gieger C, Peters A, Köttgen A, Eckardt KU, Kronenberg F. Kheirkhah A, et al. Among authors: koller a. Atherosclerosis. 2023 Dec;386:117384. doi: 10.1016/j.atherosclerosis.2023.117384. Epub 2023 Nov 10. Atherosclerosis. 2023. PMID: 37989062 Free article.
638 results